Distribution and origin of organic ligands in subsurface waters from sedimentary basins
No abstract available.
Geology topics
Publications and source records attributed to Yousif K. Kharaka.
No abstract available.
18 O values establish that waters are predominantly of meteoric origin. The chemical compositions of water and gases are controlled mainly by the ambient rock types, and chemical geothermometry gives reservoir temperatures of 80-150 degrees C indicating shallow to moderate circulation depths of up to 6 km. However, compositions and isotope abundances of noble gases and delta 13 C values of HCO 3 indicate a significant (up to 50%) mantle component for the volatiles. The relatively high fluxes of CO 2 (C/ 3 He nearly equal 10 10 ) and other volatiles of mantle origin support a deep continuous flow model, especially at depths >6 km. Numerical simulations indicate that these high fluxes of CO 2 of mantle and deep crustal origin are sufficient to generate lithostatic fluid pressures, and thus a weakened fault, in time scales comparable to those of earthquake cycles.
The U.S. Geological Survey is conducting research on the impacts of produced waters on petroleum resource development and the environment. Ongoing multidisciplinary investigations are focused on the 1) quantity and quality of current water production, 2) geologic and geochemical parameters that influence the viability of injection wells, and 3) processes that affect the dispersion of inorganic and organic constituents of produced water that are released into the surface and near-surface environment.
Groundwater brine seepage into the Dolores River in Paradox Valley, Colorado, increases the dissolved solids load of the Colorado River annually by ∼2.0 × 10 8 kg. To abate this natural contamination, the Bureau of Reclamation plans to pump ∼3540 m 3 /d of brine from 12 shallow wells located along the Dolores River. The brine, with a salinity of 250,000 mg/L, will be piped to the deepest (4.9 km) disposal well in the world and injected mainly into the Mississippian Leadville Limestone. Geochemical modeling indicates, and water-rock experiments confirm, that a huge mass of anhydrite (∼1.0 × 10 4 kg/d) likely will precipitate from the injected brine at downhole conditions of 120°C and 500 bars. Anhydrite precipitation could increase by up to 3 times if the injected brine is allowed to mix with the highly incompatible formation water of the Leadville Limestone and if the Mg in this brine dolomitizes the calcite of the aquifer. Laboratory experiments demonstrate that nanofiltration membranes, which are selective to divalent anions, provide a new technology that remediates the precipitation problem by removing ∼98% of dissolved SO 4 from the hypersaline brine. The fluid pressure used (50 bars) is much lower than would be required for traditional reverse osmosis membranes because nanofiltration membranes have a low rejection efficiency (5–10%) for monovalent anions. Our results indicate that the proportion of treatable brine increases from ∼60% to >85% with the addition of trace concentrations of a precipitation inhibitor and by blending the raw brine with the effluent stream.
No abstract available.
The solubility of the noble gases He, Ne, Ar, Kr and Xe was measured in two typical crude oils at temperatures of 25–100°C. The oil samples were obtained from the Elk Hills oil field located in southern San Joaquin Valley, California. The experimental procedure consisted of placing a known amount of gas with a known volume of crude oil in a stainless steel hydrothermal pressure vessel. The vessel was housed inside an oven and the entire unit rotates providing continuous mixing. The amount of gas dissolved in oil at a measured temperature and partial pressure of gas was used to calculate the solubility constants for these gases. Results show that the solubility of He and Ne in both oils is approximately the same; solubility then increases with atomic mass, with the solubility of Xe at 25°C being two orders of magnitude higher than that of He. The gas solubilities are somewhat higher in the lower density (higher API gravity) oil. The solubility of Ar is approximately constant in the range of temperatures of this study. The solubilities of He and Ne increase, but those of Kr and Xe decrease with increasing temperatures. Solubilities of noble gases in crude oil are significantly higher than their solubilities in water. For example, the solubilities of He and Xe at 25°C in the light oil of this study are, respectively, 3 and 24 times higher than their solubilities in pure water, and they are 15 and 300 times higher than in a brine with a salinity of 350,000 mg/l dissolved solids. These large and variable differences in the solubilities of noble gases in oil and water indicate that, in sedimentary basins with oil, these gases must be partitioned between oil, water and natural gas before they are used to deduce the origin and residence time of these fluids.
Present methods are described for the collection, preservation, and chemical analysis of waters produced from geopressured geothermal and petroleum wells. Detailed procedures for collection include precautions and equipment necessary to ensure that the sample is representative of the water produced. Procedures for sample preservation include filtration, acidification, dilution for silica, methyl isobutyl ketone (MIBK) extraction of aluminum, addition of potassium permanganate to preserve mercury, and precipitation of carbonate species as strontium carbonate for stable carbon isotopes and total dissolved carbonate analysis. Characteristics determined at the well site are sulfide, pH, ammonia, and conductivity. Laboratory procedures are given for the analysis of lithium, sodium, potassium, rubidium, cesium, magnesium, calcium, strontium, barium, iron, manganese, zinc, lead, aluminum, .and mercury by atomic absorption and flame emission spectroscopy. Chloride is determined by silver nitrate titration and fluoride by ion-specific electrode. Bromide and iodide concentrations are determined by the hypochlorite oxidation method. Sulfate is analyzed by titration using barium chloride with thorin indicator after pretreatment with alumina. Boron and silica are determined colorimetrically by the carmine and molybdate-blue methods, respectively. Aliphatic acid anions (C2 through C5) are determined by gas chromatography after separation and concentration in a chloroform-butanol mixture.